Brown Marishka K, Strus Ewa, Naidoo Nirinjini
Center for Sleep and Circadian Neurobiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Sleep. 2017 Jul 1;40(7). doi: 10.1093/sleep/zsx095.
Social isolation has a multitude of negative consequences on human health including the ability to endure challenges to the immune system, sleep amount and efficiency, and general morbidity and mortality. These adverse health outcomes are conserved in other social species. In the fruit fly Drosophila melanogaster, social isolation leads to increased aggression, impaired memory, and reduced amounts of daytime sleep. There is a correlation between molecules affected by social isolation and those implicated in sleep in Drosophila. We previously demonstrated that acute sleep loss in flies and mice induced the unfolded protein response (UPR), an adaptive signaling pathway. One mechanism indicating UPR upregulation is elevated levels of the endoplasmic reticular chaperone BiP/GRP78. We previously showed that BiP overexpression in Drosophila led to increased sleep rebound. Increased rebound sleep has also been demonstrated in socially isolated (SI) flies.
D. melanogaster were used to study the effect of social isolation on cellular stress.
SI flies displayed an increase in UPR markers; there were higher BiP levels, increased phosphorylation of the translation initiation factor eIF2α, and increased splicing of xbp1. These are all indicators of UPR activation. In addition, the effects of isolation on the UPR were reversible; pharmacologically and genetically altering sleep in the flies modulated the UPR.
The reduction in sleep observed in SI flies is a cellular stressor that results in UPR induction.
社会隔离对人类健康有诸多负面影响,包括应对免疫系统挑战的能力、睡眠量和效率,以及总体发病率和死亡率。这些不良健康后果在其他社会物种中也存在。在果蝇黑腹果蝇中,社会隔离会导致攻击性增加、记忆受损和白天睡眠时间减少。社会隔离影响的分子与果蝇睡眠相关的分子之间存在相关性。我们之前证明,果蝇和小鼠的急性睡眠剥夺会诱导未折叠蛋白反应(UPR),这是一种适应性信号通路。表明UPR上调的一种机制是内质网伴侣BiP/GRP78水平升高。我们之前表明,果蝇中BiP的过表达会导致睡眠反弹增加。在社会隔离(SI)的果蝇中也证明了反弹睡眠增加。
使用黑腹果蝇研究社会隔离对细胞应激的影响。
SI果蝇的UPR标志物增加;BiP水平更高,翻译起始因子eIF2α的磷酸化增加,xbp1的剪接增加。这些都是UPR激活的指标。此外,隔离对UPR的影响是可逆的;通过药理学和遗传学方法改变果蝇的睡眠可调节UPR。
在SI果蝇中观察到的睡眠减少是一种细胞应激源,导致UPR诱导。